This page is a drill. We take the parent topic and hit every kind of question it can throw at you: every regime of energy relative to the chemical potential, the two temperature limits, degenerate inputs, real-world numbers, and an exam-style twist. First we lay out the full grid of cases, then we work one example per cell.
Before anything, one reminder of the two objects we keep using:
Definition Two faces of Boltzmann's constant
k B
In SI units k B = 1.381 × 1 0 − 23 J/K . But electron energies are naturally in eV, so it is worth building the eV/K version once , and reusing it:
k B = 1.602 × 1 0 − 19 J/eV 1.381 × 1 0 − 23 J/K = 8.617 × 1 0 − 5 eV/K .
Why do this? Whenever an energy offset is quoted in eV, using k B in eV/K lets the eV cancel directly, with no round-trip through joules. We will call on both faces below.
Intuition What every symbol
means before we compute
Think of a shelf of energy slots stacked bottom-to-top. f answers "how full is the slot at height ε ?" — always a number between 0 (empty) and 1 (packed with its one allowed fermion). The Pauli rule is why the cap is 1 and never 2 .
Every cell below is a distinct thing the topic can test. Each numbered example targets one (or two) cells.
Intuition Reading the "Cell" labels
Each row has a short letter code so an example can announce which case it covers. A code like A∩D just uses the set-intersection symbol ∩ ("and"): it means "the situation that is both case A and case D at once" — here, sitting exactly at μ and cooling to T → 0 . No prior set theory needed; read ∩ as the word "and".
Cell
Case class
What makes it different
Example
A
ε = μ exactly
exponent is 0 ; answer is T -independent
Ex 1
B
ε > μ (above the sea)
positive exponent; f < 2 1 , decays
Ex 2
C
ε < μ (below the sea)
negative exponent; f > 2 1
Ex 2
D
T → 0 limit
step function; degenerate answer
Ex 3
A∩D
ε = μ and T → 0 (the corner)
conventional f = 2 1 by limit
Ex 1 (note)
E
High-energy tail ε − μ ≫ k B T
reduces to Maxwell-Boltzmann
Ex 4
F
Symmetry of f about μ (particle↔hole)
f ( μ + δ ) + f ( μ − δ ) = 1
Ex 5
G
Real-world density → E F , T F , v F
plug real n (sodium)
Ex 6
H
Degenerate/zero input: n → 0 or n doubled
scaling law E F ∝ n 2/3
Ex 7
I
Inverting f to find T (exam twist)
solve for the unknown temperature
Ex 8
J
Width of thermal smear ≈ 4.4 k B T
geometric read of the curve
Ex 9 (figure)
k B T energy scale at room temperature
Several examples set T = 300 K. Using the eV/K face of k B :
k B T = ( 8.617 × 1 0 − 5 eV/K ) ( 300 K ) = 0.02585 eV .
Keep this number handy — it is the natural width of thermal fuzz at room temperature.
Worked example Occupation exactly at
ε = μ
A quantum state sits at energy exactly equal to the chemical potential, at T = 300 K. What fraction of the time is it occupied? Does the answer change if T = 3000 K?
Forecast: Guess before reading — will hotter mean fuller, emptier, or no change?
Step 1. Write the exponent x = ( ε − μ ) / k B T . Since ε = μ , the numerator is 0 , so x = 0 for any T > 0 .
Why this step? The whole temperature dependence lives inside that exponent. If the numerator is zero, T cannot matter.
Step 2. Plug in: f = e 0 + 1 1 = 1 + 1 1 = 2 1 .
Why this step? e 0 = 1 exactly; this is the definitional anchor of μ .
Verify: 2 1 is dimensionless and lies in [ 0 , 1 ] ✓. It did not change with T — so the correct forecast was "no change". This is precisely how experimenters locate μ : find the energy that stays half-filled.
Intuition The corner case A∩D: what happens
exactly at ε = μ as T → 0 ?
Example 3 gives a clean step (f = 1 below, f = 0 above), but it deliberately used states 0.5 eV off the edge. Right on the edge , ε = μ , the exponent is 0/ 0 + — you must take the limit along the curve . For every T > 0 we just showed f = 2 1 , so the limiting value is lim T → 0 f ( μ ) = 2 1 . Conventionally the T = 0 step is assigned f = 2 1 at the single point ε = E F (the midpoint of the jump). It is one point of measure zero, so it never affects particle counts, but it is the correct "borderline" answer.
Worked example Two states straddling
μ
At T = 300 K take two states: one above μ by 0.05 eV, one below μ by 0.05 eV. Find f for each.
Forecast: One will be more than 2 1 , one less. Which is which, and are they related?
Step 0 (the thermal scale). From the box above, at T = 300 K, k B T = ( 8.617 × 1 0 − 5 ) ( 300 ) = 0.02585 eV.
Why this step? We will divide the eV offset by this eV energy, so both must be in eV — that is exactly what the eV/K face of k B buys us.
Step 1 (Cell B, above). x + = 0.02585 + 0.05 = 1.934 . Then f + = e 1.934 + 1 1 = 6.92 + 1 1 = 0.1263 .
Why this step? Above μ the numerator is positive, so x > 0 , so e x > 1 , so f < 2 1 : states above the sea are mostly empty.
Step 2 (Cell C, below). x − = 0.02585 − 0.05 = − 1.934 . Then f − = e − 1.934 + 1 1 = 0.1445 + 1 1 = 0.8737 .
Why this step? Below μ the numerator is negative, so e x < 1 , so f > 2 1 : states below the sea are mostly full.
Verify: f + + f − = 0.1263 + 0.8737 = 1.000 exactly. This is the particle–hole symmetry (Cell F) sneaking in: an empty slot a distance δ above μ is as likely as a filled slot δ below. Both values sit in [ 0 , 1 ] ✓.
Worked example Cold metal, sharp edge
At T = 0 , evaluate f for a state 0.5 eV below E F and a state 0.5 eV above E F .
Forecast: At absolute zero the fuzzy edge should vanish — guess the two numbers.
Step 1 (below). As T → 0 , for ε < E F the exponent ( ε − E F ) / k B T → 0 + negative → − ∞ , so e − ∞ = 0 and f = 0 + 1 1 = 1 .
Why this step? Below the Fermi energy every state is filled — the exclusion principle forces electrons to stack up rather than pile into the ground state.
Step 2 (above). For ε > E F the exponent → + ∞ , so e + ∞ = ∞ and f = ∞ + 1 1 = 0 .
Why this step? Above the sea there is nothing to fill those slots at zero temperature.
Verify: We recovered the step function: f = 1 below, f = 0 above, with the jump at E F . Consistent with Ex 1's half-filling limit approached from either side ✓ (and exactly at E F the value is 2 1 , the A∩D corner).
Worked example When Fermi-Dirac becomes classical
A state lies 0.30 eV above μ at T = 300 K. Show f is well-approximated by the Maxwell-Boltzmann form e − ( ε − μ ) / k B T , and find the relative error.
Forecast: Far up the tail, does the "+ 1 " still matter?
Step 1 — algebraic reduction. Multiply numerator and denominator of f by e − x (with x = ( ε − μ ) / k B T ):
f = e x + 1 1 = 1 + e − x e − x .
Now when x ≫ 1 , the term e − x in the denominator is tiny, so 1 + e − x → 1 and hence
f ≃ 1 e − x = e − x = e − ( ε − μ ) / k B T .
Why this step? This is the exact algebraic bridge from Fermi-Dirac to Maxwell-Boltzmann — the approximation is "drop e − x against 1 in the denominator", which is legitimate precisely because e − x is small in the high-energy tail.
Step 2 — numbers. With k B T = 0.02585 eV (same T = 300 K as before, eV/K face of k B ): x = 0.02585 0.30 = 11.60 . Then f MB = e − x = e − 11.60 = 9.14 × 1 0 − 6 , while the exact f = e 11.60 + 1 1 = 9.14 × 1 0 − 6 (agree to five figures).
Why this step? This is why classical statistics works for dilute/high-energy states — it is the ε − μ ≫ k B T limit of Fermi-Dirac.
Verify: Relative error = f f MB − f = e − x ≈ 9 × 1 0 − 6 , i.e. about 0.0009% — utterly negligible ✓.
Worked example Prove the mirror
Show that for any offset δ and any T , f ( μ + δ ) + f ( μ − δ ) = 1 .
Forecast: Ex 2 hinted at it numerically — is it exact for all δ ?
Step 1. Let y = e δ / k B T . Then f ( μ + δ ) = y + 1 1 and f ( μ − δ ) = y − 1 + 1 1 .
Why this step? Putting both onto the same base y lets us add them cleanly.
Step 2. f ( μ − δ ) = y 1 + 1 1 = 1 + y y . Add: y + 1 1 + y + 1 y = 1 + y 1 + y = 1 .
Why this step? The two fractions share a denominator once simplified, and their numerators sum to it.
Verify: Symbolically identically 1 (checked below), and it reproduces Ex 2's 0.1263 + 0.8737 = 1 ✓. Physically: the probability a state is empty at μ + δ equals the probability it is filled at μ − δ — electrons above and holes below mirror each other.
Worked example Fermi energy, temperature, velocity of sodium
Sodium has n = 2.65 × 1 0 28 m − 3 free electrons. Find E F (in eV), T F , and v F .
Forecast: Copper (parent note) gave ∼ 7 eV at n = 8.5 × 1 0 28 . Sodium is roughly 3 × less dense — guess whether E F is bigger or smaller.
Step 1 — build k F . k F = ( 3 π 2 n ) 1/3 = ( 3 ⋅ 9.8696 ⋅ 2.65 × 1 0 28 ) 1/3 = ( 7.846 × 1 0 29 ) 1/3 = 9.225 × 1 0 9 m − 1 .
Why this step? E F is cleanest through the Fermi wavevector k F ; the cube root undoes the sphere volume 3 4 π k F 3 . Keep full precision in k F — squaring it later magnifies any rounding.
Step 2 — energy in joules. E F = 2 m ℏ 2 k F 2 = 2 ( 9.11 × 1 0 − 31 ) ( 1.055 × 1 0 − 34 ) 2 ( 9.225 × 1 0 9 ) 2 = 5.20 × 1 0 − 19 J .
Why this step? ε = ℏ 2 k 2 /2 m is the free-particle energy; evaluating at k = k F gives the top of the sea. (Rounding k F to only 3 figures shifts this by a few % , so we carried the fuller value.)
Step 3 — convert to eV. Divide by the conversion factor 1 eV = 1.602 × 1 0 − 19 J :
E F = 1.602 × 1 0 − 19 J/eV 5.20 × 1 0 − 19 J = 3.24 eV .
Why this step? Joules are the SI energy; eV is the natural scale for electrons — the conversion factor is what makes the number human-readable.
Step 4 — temperature & velocity. T F = E F / k B = 1.381 × 1 0 − 23 J/K 5.20 × 1 0 − 19 J = 3.77 × 1 0 4 K . v F = ℏ k F / m = 9.11 × 1 0 − 31 ( 1.055 × 1 0 − 34 ) ( 9.225 × 1 0 9 ) = 1.068 × 1 0 6 m/s .
Why this step? T F tells us how degenerate the gas is (T F ≫ 300 K ⇒ deeply degenerate); v F is the speed of electrons at the sea surface. Note we use E F in joules here so it cancels the joules in k B .
Verify: Units: J / ( J/K ) = K ✓; v F is ∼ 0.4% of light speed (non-relativistic, so free-electron formula is valid) ✓. Lower density than copper ⇒ lower E F (3.24 < 7 eV), matching the E F ∝ n 2/3 scaling — correct forecast. (Standard tables quote sodium E F ≈ 3.24 eV.)
Worked example Scaling and edge cases
(a) If you double the electron density n → 2 n at fixed volume, by what factor does E F change? (b) What is E F in the limit n → 0 ?
Forecast: E F ∝ n 2/3 . Doubling n — factor bigger than 2 or smaller?
Step 1 (a). E F ( n ) E F ( 2 n ) = ( n 2 n ) 2/3 = 2 2/3 = 1.587 .
Why this step? Only the density enters E F , and it does so as the 3 2 power; the constants cancel in the ratio.
Step 2 (b). As n → 0 , E F = const ⋅ n 2/3 → 0 .
Why this step? An empty box has no Fermi sea — the top of a non-existent stack is at zero energy. This is the degenerate/zero-input check the matrix demanded.
Verify: 2 2/3 = 1.587 < 2 — smaller than doubling, because the exponent is below 1 (correct forecast). And n → 0 ⇒ E F → 0 is finite and sensible ✓.
Worked example Given the occupation, find
T
A state 0.10 eV above μ is observed to have occupation f = 0.20 . What temperature is the system at?
Forecast: More thermal smearing (higher T ) pushes f at a fixed offset closer to 2 1 . Since 0.20 < 2 1 , guess: is T small or large?
Step 1 — invert f . From f = e x + 1 1 : e x = f 1 − 1 = 0.20 1 − 1 = 4 , so x = ln 4 = 1.386 .
Why this step? We know the output f and want the input x ; algebraically isolating e x then taking ln is the inverse of the distribution.
Step 2 — solve for T . x = k B T ε − μ ⇒ T = k B x ε − μ = ( 8.617 × 1 0 − 5 eV/K ) ( 1.386 ) 0.10 eV = 837 K .
Why this step? We use k B in eV/K (the face we built at the top, 8.617 × 1 0 − 5 ) so the eV in the numerator cancels, leaving kelvin.
Verify: Plug back: x = ( 0.10 ) / ( 8.617 × 1 0 − 5 ⋅ 837 ) = 1.386 , and f = 1/ ( e 1.386 + 1 ) = 1/ ( 4 + 1 ) = 0.20 ✓. This T is well below T F , consistent with a mostly-empty state above μ .
Worked example How wide is the fuzzy edge?
At T = 1000 K, over what energy width does f fall from 0.90 to 0.10 ? Read it off the curve.
Forecast: The parent note claims ≈ 4.4 k B T . Guess the width in eV first.
How to read the figure: the thick blue S-shaped curve is f plotted against the scaled energy x = ( ε − μ ) / k B T . The vertical dashed gray line marks ε = μ (x = 0 ), where the gray dot sits at the half-filled value f = 0.5 . The two round orange markers on the curve's shoulders sit at f = 0.90 (upper-left) and f = 0.10 (lower-right); these are the two occupation levels the question asks about. The green horizontal double-headed arrow with its shaded band spans the horizontal distance between those two markers — that span is the width we want, measured in units of k B T .
Step 1 — the two edge exponents. f = 0.90 ⇒ e x = 0.9 1 − 1 = 0.111 ⇒ x = ln ( 0.111 ) = − 2.197 . f = 0.10 ⇒ e x = 9 ⇒ x = + 2.197 .
Why this step? These x values are exactly the horizontal positions of the two orange shoulder markers in the figure. Their span in x is 2.197 − ( − 2.197 ) = 4.394 — the length of the green band.
Step 2 — convert to energy. The width in scaled units is Δ x = 4.394 , so Δ ε = 4.394 k B T . With k B T = ( 8.617 × 1 0 − 5 eV/K ) ( 1000 K ) = 0.0862 eV: Δ ε = 4.394 × 0.0862 = 0.379 eV.
Why this step? x is measured in units of k B T , so multiplying the x -span (the band's length) by k B T converts the "shoulder width" from dimensionless to eV. This is the quantitative read-off the figure was set up to deliver.
Verify: 4.394 ≈ 4.4 , matching the parent note's 4.4 k B T claim ✓. Numerically Δ ε = 0.379 eV at 1000 K. In a metal with E F ∼ 3 –7 eV this 0.38 eV smear is a thin sliver near the top — only electrons in that band are thermally/electrically active. Units: (dimensionless)×eV = eV ✓, closing cell J.
Recall Quick self-test
A state at ε − μ = − k B T has what occupation? ::: f = 1/ ( e − 1 + 1 ) = 1/1.368 = 0.731
If f = 0.5 and ε > 0 , where is μ ? ::: exactly at ε (Cell A)
Doubling n multiplies E F by? ::: 2 2/3 ≈ 1.587 (Cell H)
The high-energy tail of f reduces to which classical law? ::: Maxwell-Boltzmann e − ( ε − μ ) / k B T (Cell E)
Mnemonic The whole page in one breath
"Below full, above empty, μ is fifty-fifty, and the edge is 4.4 k B T wide."
See also: Density of States (turns f into particle numbers), Sommerfeld Expansion (how μ drifts from E F at finite T ), and Electron Degeneracy Pressure & White Dwarfs (what the filled sea holds up).